autosomal recessive limb-girdle muscular dystrophy type 2G
autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the gene encoding telethonin (TCAP)
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autosomal recessive limb-girdle muscular dystrophy type 2G
Summary
autosomal recessive limb-girdle muscular dystrophy type 2G is a rare disease[1].
Key Facts
- autosomal recessive limb-girdle muscular dystrophy type 2G's instance of is recorded as rare disease[2].
- autosomal recessive limb-girdle muscular dystrophy type 2G's instance of is recorded as class of disease[3].
- autosomal recessive limb-girdle muscular dystrophy type 2G's subclass of is recorded as autosomal recessive limb-girdle muscular dystrophy[4].
- autosomal recessive limb-girdle muscular dystrophy type 2G's subclass of is recorded as qualitative or quantitative defects of telethonin[5].
- autosomal recessive limb-girdle muscular dystrophy type 2G's MeSH descriptor ID is recorded as C566599[6].
- autosomal recessive limb-girdle muscular dystrophy type 2G's OMIM ID is recorded as 601954[7].
- autosomal recessive limb-girdle muscular dystrophy type 2G's Disease Ontology ID is recorded as DOID:0110281[8].
- autosomal recessive limb-girdle muscular dystrophy type 2G's Orphanet ID is recorded as 34514[9].
- autosomal recessive limb-girdle muscular dystrophy type 2G's health specialty is recorded as neurology[10].
- autosomal recessive limb-girdle muscular dystrophy type 2G's genetic association is recorded as TCAP[11].
- autosomal recessive limb-girdle muscular dystrophy type 2G's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110281[12].
- autosomal recessive limb-girdle muscular dystrophy type 2G's exact match is recorded as http://identifiers.org/doid/DOID:0110281[13].
- autosomal recessive limb-girdle muscular dystrophy type 2G's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_34514[14].
- autosomal recessive limb-girdle muscular dystrophy type 2G's UMLS CUI is recorded as C1866008[15].
- autosomal recessive limb-girdle muscular dystrophy type 2G's ICD-10-CM is recorded as G71.0[16].
- autosomal recessive limb-girdle muscular dystrophy type 2G's GARD rare disease ID is recorded as 10471[17].
- autosomal recessive limb-girdle muscular dystrophy type 2G's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- autosomal recessive limb-girdle muscular dystrophy type 2G's Mondo ID is recorded as MONDO_0011170[19].